F Giraud

2.7k citations
129 papers · 2.2k · h-index 26

Impact in

  • Genetics top 1%
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Prenatal Screening and Diagnostics

Papers in

    • Genomic variations and chromosomal abnormalities 27
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 10
    • Genetics and Neurodevelopmental Disorders 10

F Giraud

120 papers receiving 2.0k citations

Peers

F Giraud
Comparison fields: 5 of 112
  • Genetics 1.1k
  • Pediatrics, Perinatology and Child Health 353
  • Developmental Biology 37
  • Molecular Biology 895
  • Clinical Biochemistry 82
Replace U. Claussen with:
U. Claussen Germany
Gerald L. Feldman United States
George H. Thomas United States
Philippe Bouchard France
Janice Smith United States
Colleen Jackson‐Cook United States
ELIZABETH B. ROBSON United Kingdom
Ebba U. Kurz Canada
Roy A. Gravel Canada
Dominic J. Smiraglia United States
F Giraud relative to U. Claussen Germany U. Claussen's profile →
Citations per field
00.5×5.1×
U. Claussen · 1×
Citations per year

Countries citing papers authored by F Giraud

Since Specialization
Citations

This map shows the geographic impact of F Giraud's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by F Giraud with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F Giraud more than expected).

Fields of papers citing papers by F Giraud

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F Giraud. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by F Giraud. The network helps show where F Giraud may publish in the future.

Co-authors

The 25 scholars most cited alongside F Giraud, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with F Giraud Line = papers co-authored together F Giraud links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 129 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1982132
2 1976117
3 201197
4 198981
5 198171
6 198167
7 198367
8 198163
9 197661
10 198953
11 197946
12 200642
13 198142
14 200840
15 198140
16 199537
17 201635
18 197934
19 200833
20 199132

About F Giraud

F Giraud is a scholar working on Genetics, Molecular Biology, Organic Chemistry, Pediatrics, Perinatology and Child Health and Pathology and Forensic Medicine, having authored 129 papers that have together received 2.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (27 papers), Synthesis and biological activity (14 papers), Prenatal Screening and Diagnostics (14 papers), Cancer Mechanisms and Therapy (11 papers), Chromosomal and Genetic Variations (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Synthesis and Biological Evaluation (9 papers). The work is most often cited by research in Genetics (1.1k citations), Pediatrics, Perinatology and Child Health (353 citations), Developmental Biology (37 citations), Molecular Biology (895 citations) and Clinical Biochemistry (82 citations). F Giraud has collaborated with scholars based in France, Norway and Russia. Frequent co-authors include Marie‐Geneviève Mattéi, J. F. Mattéi, Ségolène Aymé, Pascale Moreau, Fabrice Anizon, Isabel Ferreirós-Vidal, Lionel Nauton, Vincent Théry, Marc Le Borgne and Y Aurran. Their work appears in journals such as Human Genetics, European Journal of Medicinal Chemistry, Clinical Genetics, Bioorganic & Medicinal Chemistry Letters and Journal of Medical Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact